DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
LYOPHILIZED CYTOXAN
FDA Application No:
(NDA) 012142
Active Ingredient(s):
CYCLOPHOSPHAMIDE
Company:
BRISTOL MYERS SQUIBB
Original Approval or Tentative Approval Date:
November 16, 1959
Chemical Type:
2 New active ingredient
Review Classification:
P Priority review drug
Therapeutic Equivalents
Label Information
Approval History, Letters, Reviews and Related Documents
You can see the products in the same application. The table can be sorted by clicking the header columns.
Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
CYTOXAN
CYCLOPHOSPHAMIDE
100MG/VIAL
INJECTABLE; INJECTION
Discontinued
No
None
CYTOXAN
CYCLOPHOSPHAMIDE
200MG/VIAL
INJECTABLE; INJECTION
Discontinued
No
None
CYTOXAN
CYCLOPHOSPHAMIDE
500MG/VIAL
INJECTABLE; INJECTION
Discontinued
No
None
CYTOXAN
CYCLOPHOSPHAMIDE
1GM/VIAL
INJECTABLE; INJECTION
Discontinued
No
None
CYTOXAN
CYCLOPHOSPHAMIDE
2GM/VIAL
INJECTABLE; INJECTION
Discontinued
No
None
LYOPHILIZED CYTOXAN
CYCLOPHOSPHAMIDE
100MG/VIAL
INJECTABLE; INJECTION
Prescription
Yes
AP
LYOPHILIZED CYTOXAN
CYCLOPHOSPHAMIDE
200MG/VIAL
INJECTABLE; INJECTION
Prescription
Yes
AP
LYOPHILIZED CYTOXAN
CYCLOPHOSPHAMIDE
500MG/VIAL
INJECTABLE; INJECTION
Prescription
Yes
AP
LYOPHILIZED CYTOXAN
CYCLOPHOSPHAMIDE
2GM/VIAL
INJECTABLE; INJECTION
Prescription
Yes
AP
LYOPHILIZED CYTOXAN
CYCLOPHOSPHAMIDE
1GM/VIAL
INJECTABLE; INJECTION
Prescription
Yes
AP
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